Team Meg!

This project was started in the summer of 2014 in efforts to raise a good amount of money for Meg's surgery. Meg, 17, who lives in West Yorkshire, England, suffers from a rare disease called Ehlers-Danlos Syndrome (EDS for short). EDS is a connective tissue disorder that can cause hypermobility of the joints and skin, easily bruised skin and broken bones, cerebral relapse, the inability to walk and sit upright, and extreme pain. Meg needs her surgery in order to survive. So I'm asking you to donate at least $5. ALL of the money riased is going directly to Meg and her family. As of October, 2015, we have raised close to $18,000. I am hoping to raise a lot more. UPDATE: The money will be going to her physio leading up to and after a surgery planned for May by Dr. Henderson for a tethered cord. Thank you.